Fusarium solani

FDA Drug Profile — Fusarium, Fusarium solani

Drug Details

Generic Name
Fusarium solani
Brand Names
Fusarium, Fusarium solani
Application Number
BLA102211
Sponsor
Allermed Laboratories, Inc.
NDC Codes
5
Dosage Forms
INJECTION, SOLUTION
Routes
CUTANEOUS, INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS
Active Ingredients
HAEMATONECTRIA HAEMATOCOCCA

Indications and Usage

USES: May help temporarily relieve allergy symptoms ■ headache ■ itchy, watery eyes ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: Stop use and ask a doctor if ■ symptoms do not improve in 5 days or new symptoms appear ■ you are an asthma sufferer with severe mold allergies If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)